IRF6 is a mediator of Notch pro-differentiation and tumour suppressive function in keratinocytes.


Autoria(s): Restivo G.; Nguyen B.C.; Dziunycz P.; Ristorcelli E.; Ryan R.J.; Özuysal Ö.Y.; Di Piazza M.; Radtke F.; Dixon M.J.; Hofbauer G.F.; Lefort K.; Dotto G.P.
Data(s)

2011

Resumo

While the pro-differentiation and tumour suppressive functions of Notch signalling in keratinocytes are well established, the underlying mechanisms remain poorly understood. We report here that interferon regulatory factor 6 (IRF6), an IRF family member with an essential role in epidermal development, is induced in differentiation through a Notch-dependent mechanism and is a primary Notch target in keratinocytes and keratinocyte-derived SCC cells. Increased IRF6 expression contributes to the impact of Notch activation on growth/differentiation-related genes, while it is not required for induction of 'canonical' Notch targets like p21(WAF1/Cip1), Hes1 and Hey1. Down-modulation of IRF6 counteracts differentiation of primary human keratinocytes in vitro and in vivo, promoting ras-induced tumour formation. The clinical relevance of these findings is illustrated by the strikingly opposite pattern of expression of Notch1 and IRF6 versus epidermal growth factor receptor in a cohort of clinical SCCs, as a function of their grade of differentiation. Thus, IRF6 is a primary Notch target in keratinocytes, which contributes to the role of this pathway in differentiation and tumour suppression.

Identificador

http://serval.unil.ch/?id=serval:BIB_6437DA9C05EF

isbn:1460-2075 (Electronic)

pmid:21909072

doi:10.1038/emboj.2011.325

isiid:000297691500006

Idioma(s)

en

Fonte

Embo Journal, vol. 30, no. 22, pp. 4571-4585

Tipo

info:eu-repo/semantics/article

article